- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04549961
123 nutritionDay in Worldwide ICUs: An International Audit and Registry on Nutrition and Outcome.
The aim of this project is to increase knowledge and awareness about nutrition of ICU patients among the staff by evaluating nutrition care on an international level. In order to be able to facilitate bench-marking of ICU's with a national and international standard and actual best practice, we intend to provide a multi-lingual data acquisition tool to determine actual nutrition care in an ICU's.
nutritionDay in Worldwide ICUs is a one day international cross-sectional audit.
Study Overview
Detailed Description
One day international cross-sectional audit in all types of intensive care units. Data are collected with the help of questionnaires. Anonymised data entry into the audit database is done with individual and anonymous center and unit-codes.
There are 4 questionnaires to be completed on nutritionDay.
- Unit Sheet: asks for nutrition related organisational and structural information on the ward.
- Patient Medical Information Admission Day: asks for patients status (gender/age/weight/height etc.), date of ICU admission and laboratory parameters on admission day.
- Patient Medical Information Actual Day: includes questions about treatment (insulin therapy/antibiotic treatment, etc.) and laboratory parameters on actual day.
- Patient Nutrition: comprises questions about enteral and parenteral nutrition. Number of days of parenteral/enteral feeding, planned amount of calories per day and the patients well being.
Outcome Evaluation: re-assesses the patient's outcome 60 days after nutritionDay (discharged, still in hospital, transferred, death...).
Participation rules:
A user needs to register to nutritionDay as a member to the nutritionDay network. Each may choose a personal user name. Each user needs to provide a valid email address. After responding to a validation email the user is registered with the chosen user name. User details are stored on a system that is not connected to the nutritionDay registry at any time. One user may serve as contact for several units and centers.
A user may order codes for participation for one or several centers and units. Access to the registry is only possible with a center code and unit code. These codes are selected from a list of random numbers.
Audit/registry recruitment plan:
Participation to the registry is voluntary. There is actually no participation fee. All necessary information can be obtained from a dedicated website (www.nutritionday.org). Participation can be promoted via international and national scientific societies, universities, health care organisations or governmental agencies as well as via advertisement at international and national congresses. The target would be intensive care units within hospitals of different sizes and level of care.
Risk and benefit assessment:
The benefit for each patient is that awareness and knowledge about nutrition related factors and treatment options in the treating unit is increased. There is no individual risk since the audit is purely observational.
The benefit for the individual unit is to receive an extensive benchmarking report displaying the unit data in comparison with all units from the same specialty from the previous 3 years immediately after the end of data entry and a validation step. Units or groups of units may request specific reports that can be obtained only after a case by case agreement and financial coverage. All data used as a reference for benchmarking purpose are from units where a minimum of 60% of actually present patients have been recruited and the outcome at day 60 is available in more than 80% of these patients. There is no risk for the unit since anonymity of unit is structurally strictly maintained.
The benefit for the registry up-to-date data enabling benchmarking in pace with medical and care evolution. Moreover the registry data are used for research of the scientific community.
Data security:
On the datasheets the unit and the hospital/center are identified by a numeric code delivered after application to the nutritionDay coordinating center by an automatic system. The only requirement is a valid email address for direct communication with the unit.
Patients are usually identified on the locally used questionnaires by initials and age, but use of initials is not mandatory. Consecutive numbering is also possible. Only the participating unit has to trace patients identifier to be able to collect hospital outcome at day 60 after nutritionDay and to answer automatic requests for data clarification during the data quality feedback.
During data entry into the electronic registry only anonymous codes for center, unit and patients are possible. Thus the data handling centre cannot trace data back to an individual patient. The access to data entry is protected by anonymous center-code and unit-code.
Typically all data are collected via a dedicated website accessed via www.nutritionday.org .
The protected data server is run by the Center for Medical Statistics Informatics and Intelligent Systems (CEMSIS) of the Medical University Vienna. The data server is mirrored and backed up. The data server is protected within the University Firewall against external access.
Data feedback and individual unit report
All participating units are entitled to receive a bench-marking report from the registry. The report generator is started by the participating unit, when data entry has been completed. As a first step each unit receives a data feedback sheet that is based on an electronic data plausibility and missing data analysis. After stating that all data are correctly entered the final report can be generated. This final report offers complete descriptive statistics of the unit data compared to the reference data from the previous 4 years of the corresponding specialty. Only data from units fulfilling a high data quality standard are used for the reference. More than 60% of the patients present in the unit need to participate and 80% of these patients need to have their outcome recorded. Optionally the period used for comparison can be extended until 2007. All descriptive statistics represent prevalent data and are not corrected for cross-sectional sampling to allow direct data control and interpretation.
All downloaded reports of a unit are consecutively numbered and stored for documentation purpose.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Silvia Tarantino, Dr.
- Phone Number: +436805524917
- Email: office@nutritionday.org
Study Locations
-
-
-
Vienna, Austria, 1090
- Recruiting
- Medical University Vienna, CEMSIIS
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients admitted to an intensive care unit on nutritionDay
- patients aged 6 and older
Exclusion Criteria:
- refusal of patient or relatives to participate in nutritionDay
- patient aged 5 and under
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
patients admitted to intensive care units
all patients that are present on an intensive care unit on nutritionday
|
type and amount of food eaten or type and amount of oral nutritional supplements as well as enteral or parenteral nutrition
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
60 day hospital mortality
Time Frame: 60 days
|
death within 60 days of sampling day
|
60 days
|
Length of ICU stay
Time Frame: 60 days
|
difference in days between ICU admission and ICU discharge
|
60 days
|
Route of nutrition
Time Frame: at nutritionDay (the sampling day)
|
artificial nutrition is defined in 4 categories (yes/no):
|
at nutritionDay (the sampling day)
|
planned and delivered amount of nutrition
Time Frame: 24 hour period before nutritionDay and 24 hour period of nutritionDay (the sampling day)
|
amount of nutrition in kilocalories from all routes:
|
24 hour period before nutritionDay and 24 hour period of nutritionDay (the sampling day)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Structural parameters: number of ICU beds
Time Frame: baseline ( on the day of cross-sectional data collection nutritionDay)
|
number of staffed ICU beds
|
baseline ( on the day of cross-sectional data collection nutritionDay)
|
Structural parameter: human resources
Time Frame: baseline ( on the day of cross-sectional data collection nutritionDay)
|
number of physician, nurses, dietician present in the ICU during the morning shift
|
baseline ( on the day of cross-sectional data collection nutritionDay)
|
Collaborators and Investigators
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 509/2006 (ICU)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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